Linked Data
gnomAD v4:
10-110644312-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110644312C>A , CM000672.2:g.110644312C>A | GRCh38 |
| NC_000010.10:g.112404070C>A , CM000672.1:g.112404070C>A | GRCh37 |
| NC_000010.9:g.112394060C>A | NCBI36 |
| NG_021177.1:g.4916C>A , LRG_382:g.4916C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017016103.2:c.26+872C>A | XP_016871592.1:n.26+872C>A |